» Articles » PMID: 4982204

An Electron Microscopic Characterization of Classes of Synaptic Vesicles by Means of Controlled Aldehyde Fixation

Overview
Journal J Cell Biol
Specialty Cell Biology
Date 1970 Jan 1
PMID 4982204
Citations 37
Authors
Affiliations
Soon will be listed here.
Abstract

Examination of variables of aldehyde fixation that may affect the shape of agranular synaptic vesicles has revealed that even brief storage of aldehyde-perfused nervous tissue pieces in cacodylate buffer, prior to hardening in osmium tetroxide, has an unusually severe flattening effect on agranular vesicles of a particular type. These are the vesicles of peripheral cholinergic axon endings, and of certain central synaptic bulbs. Types of synaptic bulbs can now be further defined on the basis of shape of agranular synaptic vesicles under controlled conditions of aldehyde fixation. Previously described "S" bulbs in the spinal cord contain uniformly spheroid vesicles, which are wholly resistant to flattening. Previously described "F" bulbs contain somewhat smaller agranular vesicles that are flattened after aldehyde fixation, even when this is followed by prompt hardening in osmium tetroxide solution. A third type, previously characterized as having irregularly round agranular vesicles after the above treatment, contains only severely flattened vesicles when the osmium tetroxide hardening is preceded by even a brief wash with sodium cacodylate buffer containing sucrose. Moreover, the "third" type is characteristic of all cholinergic peripheral axon endings examined, as well as the large axosomatic ("L") synaptic bulbs of the spinal cord.

Citing Articles

High-resolution volumetric imaging constrains compartmental models to explore synaptic integration and temporal processing by cochlear nucleus globular bushy cells.

Spirou G, Kersting M, Carr S, Razzaq B, Yamamoto Alves Pinto C, Dawson M Elife. 2023; 12.

PMID: 37288824 PMC: 10435236. DOI: 10.7554/eLife.83393.


Partial connectomes of labeled dopaminergic circuits reveal non-synaptic communication and axonal remodeling after exposure to cocaine.

Wildenberg G, Sorokina A, Koranda J, Monical A, Heer C, Sheffield M Elife. 2021; 10.

PMID: 34965204 PMC: 8716107. DOI: 10.7554/eLife.71981.


Pleomorphic linkers as ubiquitous structural organizers of vesicles in axons.

Schrod N, Vanhecke D, Laugks U, Stein V, Fukuda Y, Schaffer M PLoS One. 2018; 13(6):e0197886.

PMID: 29864134 PMC: 5986143. DOI: 10.1371/journal.pone.0197886.


Characterization of early pathogenesis in the SOD1(G93A) mouse model of ALS: part I, background and methods.

Vinsant S, Mansfield C, Jimenez-Moreno R, Gaizo Moore V, Yoshikawa M, Hampton T Brain Behav. 2014; 3(4):335-50.

PMID: 24381807 PMC: 3869677. DOI: 10.1002/brb3.143.


Synaptic plasticity in the medial superior olive of hearing, deaf, and cochlear-implanted cats.

Tirko N, Ryugo D J Comp Neurol. 2012; 520(10):2202-17.

PMID: 22237661 PMC: 3963361. DOI: 10.1002/cne.23038.


References
1.
Nadol Jr J, DE LORENZO A . Observations on the abdominal stretch receptor and the fine structure of associated axo-dendritic synapses and neuromuscular junctions in homarus. J Comp Neurol. 1968; 132(3):419-43. DOI: 10.1002/cne.901320305. View

2.
Graham Jr L, Shank R, WERMAN R, Aprison M . Distribution of some synaptic transmitter suspects in cat spinal cord: glutamic acid, aspartic acid, gamma-aminobutyric acid, glycine and glutamine. J Neurochem. 1967; 14(4):465-72. DOI: 10.1111/j.1471-4159.1967.tb09545.x. View

3.
BODIAN D, Taylor N . Synapse Arising at Central Node of Ranvier, and Note on Fixation of the Central Nervous System. Science. 1963; 139(3552):330-2. DOI: 10.1126/science.139.3552.330. View

4.
Karnovsky M . The ultrastructural basis of capillary permeability studied with peroxidase as a tracer. J Cell Biol. 1967; 35(1):213-36. PMC: 2107108. DOI: 10.1083/jcb.35.1.213. View

5.
BODIAN D . AN ELECTRON-MICROSCOPIC STUDY OF THE MONKEY SPINAL CORD. I. FINE STRUCTURE OF NORMAL MOTOR COLUMN. II. EFFECTS OF RETROGRADE CHROMATOLYSIS. III. CYTOLOGIC EFFECTS OF MILD AND VIRULENT POLIOVIRUS INFECTION. Bull Johns Hopkins Hosp. 1964; 114:13-119. View